Canonical Allele Identifier: CA2619691029
Gene: HMGA2 HGNC NCBI

Linked Data

gnomAD v4: 12-65965928-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65965928A>G , CM000674.2:g.65965928A>G GRCh38
NC_000012.11:g.66359708A>G , CM000674.1:g.66359708A>G GRCh37
NC_000012.10:g.64645975A>G NCBI36
NG_016296.1:g.146469A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.*2636A>G MANE Select ENSP00000384026.2:n.*2636A>G
ENST00000403681.6:c.*2636A>G ENSP00000384026.2:n.*2636A>G
NM_003483.4:c.*2636A>G NP_003474.1:n.*2636A>G
NM_003483.6:c.*2636A>G MANE Select NP_003474.1:n.*2636A>G
Search 100 bp 5'
Search 100 bp 3'